Variant (rsID / SNP)
rs1800899
rs1800899 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to TP53. Location: chromosome 17, position 7,576,841. Clinical significance in the table: Benign/Likely benign.
Reference-table entries
TP53Benign
- Clinical significance (as recorded)
- Benign/Likely benign
- Variant type
- single nucleotide variant
- Chromosome / position
- 17:7576841
- Cytoband
- 17p13.1
- HGVS
- NM_000546.6(TP53):c.993+12T>C
- Allele change
- Silent
Associated conditions / phenotypes
Hereditary cancer-predisposing syndrome|Li-Fraumeni syndrome 1|Malignant tumor of breast|Li-Fraumeni syndrome|Breast and/or ovarian cancer|Hereditary breast ovarian cancer syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.